期刊文献+

对溴苯异氰酸酯的合成研究 被引量:2

Synthesis of 4-Bromophenyl Isocyanate
下载PDF
导出
摘要 研究以对溴苯胺和三光气为原料合成对溴苯异氰酸酯,重点讨论溶剂、反应温度、反应时间和原料配比等对合成工艺的影响。研究表明:以乙酸乙酯为溶剂,滴液温度-5~0℃,回流温度78℃,反应时间为5.0 h,三光气∶对溴苯胺=1∶2(摩尔比),对溴苯异氰酸酯的收率可达90.4%。 4-Bromophenyl isocyanate was prepared from triphosgene and 4-bromoaniline.The effects of solvents,reaction temperature,reaction time and the mole ratio of raw materials on the yield of 4-bromophenyl isocyanate were studied.The optimum reaction conditions were obtained as follows: the solvent ethyl acetate,titration temperature-5~0℃,the refluxing temperature 78℃,the mole ratio of 4-bromoaniline to triphosgene 2∶1 and reaction time 4.5 h.The results of parallel tests showed that under such optimum condition the yield of 4-bromophenyl isocyanate could reach 90.4%.
作者 施成进
出处 《丽水学院学报》 2010年第5期30-32,共3页 Journal of Lishui University
关键词 对溴苯异氰酸酯 三光气 对溴苯胺 合成 4-bromophenyl isocyanate triphosgene 4-bromoaniline synthesis
  • 相关文献

参考文献6

二级参考文献53

  • 1谭成侠,翁建全,孙娜波,沈德隆.2-二乙胺基-6-甲基-4-羟基嘧啶的合成[J].农药,2005,44(6):261-262. 被引量:7
  • 2陈馥衡,王红军.一些二唑类与三唑类化合物的合成及其生物活性的研究[J].应用化学,1989,6(4):38-45. 被引量:2
  • 3Yoshitakia Matsushima,Takuyu Nakayama,Shigehiro Tohyama,et al. Versatile route to 2,6-dideocyamino sugars from non-sugar materials: synthesis of vicenisamine and kedarosammine [J]. J.Chem. Soc. Perkin Trans. 1. 2001 (6): 569 - 577.
  • 4David $.Brown, Mark C. Elliott, Christoper J. Moody, et al.Ligand effects in the rhodium (Ⅱ)-catalyzed reaction of diazo-mides oxindole formation is promoted by the use of rhodium (Ⅱ)perfluorocarboxamide catalysts [J]. J. Org. Chem. [J],1994,59(9) :2447
  • 5Qingmin Wang, Runqiu Hung. Synthesis and biological activity of novel N/-terbutyl-N/-substituted berzoyl-N-(substituted phenyl)aminocarbonylhydrazines and their derivatives [J] .Tetrahedron Lett., 2001,42: 8881-8883.
  • 6Heiner Eckert, Barbara Forster. Triphosgene, a crystalline phosgene substitute [J] . Chem. Int. Ed. Engl, 1987, 26 (9): 894-895.
  • 7Remigiusz Kocz, Juliatiek Roeslamadji, Shahriar Mobashery. A convenient triphosgene-mediated synthesis of symmetric carboxylic acid anhydrides [J]. J. Org. Chem.. 1994,59 (20): 2913-2914.
  • 8I. A. Rivero, S. Heredia, A. Ochoa. Etherification of amino acid and monoacids using triphosgene [J]. Synth. Commun. 2001,31 (14) :2169-2175.
  • 9Sabrina Castellano, Giorgio Stefancioh. Synthesis of tricyclic triazepinones related to nevirapine [J] .J.Hetercyclic Chem.. 2000, 37:1539-1542.
  • 10Quan Zhang, ChongSheng Shi, Hai-Ren Zhang, et al. Synthesis of OH-indolo [2.3.-b] [1.6] naphthyridines of ellipticine alkaloids [J].J.Org.Chem.,2000,65(23):7977-7983.

共引文献43

同被引文献12

  • 1刘强,曹桂荣,魏文珑,常宏宏,王志忠.异氰酸酯化合物的研究进展[J].山西化工,2007,27(5):28-32. 被引量:8
  • 2Yu K, Shi C, Toral BL, et al. Beyond rapalog therapy: preclini- cal pharmacology and antitumor activity of WYE-125132, an ATP- competitive and specific inhibitor of mTORC1 and mTORC2[ Jl. Cancer Res, 2010,70(2) :621 -631.
  • 3Curran K J, Verheijen JC, Kaplan J, et al. Pyrazolopyrimidines as highly potent and selective, ATP-competitive inhibitors of the mammalian target of rapamycin ( mTOR ) : optimization of the 1- substituent[J]. Bioorg Med Chem Lett, 2010,20(4):1440 -1444.
  • 4Yu K, Toral BL, Shi C, et al. Biochemical, cellular, and in vivo activity of novel ATP-competitive and selective inhibitors of the mammalian target of rapamycin [ J ]. Cancer Res, 2009,69 ( 15 ) : 6232 - 6240.
  • 5Zask A, Koplan A, Verheijen JC, et al. Thienopyrimidine and pyrazolopyrimidine compounds and their use as mTOR kinase and PI3 kinase inhibitors:US,US8129371 [ P]. 2012 -05 -06.
  • 6Artigas G, MarchOn V. Synthesis of Janus compounds for the recognition of G-U mismatched nucleobase pairs[J]. J Org Chem, 2013,78(21 ) :10666 - 10677.
  • 7Wang J, Liang YL, Qu J. Boiling water-catalyzed neutral and selective N-Boc deprotection [ J ]. Chem Commun, 2009, ( 34 ) : 5144 - 5146.
  • 8Yoshihiko N, Nobuaki S, Yuki I, et al. Pyridinylpyrazoloquino- line eornponnd : Japan, WO2014163146 [ P ]. 2014 - 10 - 09.
  • 9齐庆莹.固体光气法合成3,4-二甲氧基苯异氰酸酯[J].精细化工中间体,2008,38(2):35-37. 被引量:6
  • 10高俊杰,李会泉,张懿,费维扬.MDI清洁合成工艺研究进展[J].化工进展,2009,28(2):309-315. 被引量:7

引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部